Int'l Conference on Gene Editing and CRISPR Technologies (GECT 2022) 

Conference Date: May 27-29, 2022Conference Venue: Xi'an, ChinaWebsite: https://www.maymeeting.org/conference/GECT2022/Online Registration System: https://www.maymeeting.org/RegistrationSubmission/default.aspx?ConferenceID=1479Email: wsconf5@163.com

Int'l Conference on Gene Editing and CRISPR Technologies (GECT 2022) will be held in Xi'an, China, during May 27-29, 2022. The aim of GECT is to provide a stage for researchers, engineers, academicians as well as industrial professionals from all over the world to present their research results and development activities in Biomedicine, Clinical Application of Gene Editing, CRISPR Systems and CRISPR Technologies, Effective Delivery for Genes in Vitro, Gene Knock In and Genomic Screening, Genome Engineering and DNA repair, Single Base Editing, etc. GECT 2022 will be a valuable and important platform for inspiring international and interdisciplinary exchange at the forefront of CGene Editing and CRISPR Technologies. 

If you wish to serve the conference as an invited speaker, please send email to us with your CV. We'll contact with you asap.

Publication and Presentation

Publication: Open Access Journal，please contact us for detailed informationIndex: CNKI and Google ScholarNote: If you want to present your research results but do NOT wish to publish a paper, you may simply submit an Abstract to our Registration System.

Contact Us

Email: wsconf5@163.comTel: +86 132 6470 2250 (From Monday to Friday)QQ: 1349406763 WeChat: 3025797047Official Account: Academic Communications

Attendance Methods

1.Submit full paper (Regular Attendance+Paper Publication+Presentation)You are welcome to submit full paper, all the accepted papers will be published by Open access journal.2. Submit abstract (Regular Attendance+Abstract+Presentation)3. Regular Attendance (No Submission Required) 

Conference Topics

BiomedicineCas Genes and CRISPR SubtypesClinical Application of Gene EditingCRISPR BiologyCRISPR Systems and CRISPR TechnologiesCRISPR-Associated SystemsDelivery and specificity of CRISPR-based toolsDifferent Gene Delivery SystemsDisease ModelsEffective Delivery for Genes in VitroGene DriveGene Editing Technology and Gene Editing EfficiencyGene Editing-Based Safety and EthicsGene FunctionGene Knock In and Genomic ScreeningGene TherapyGenetic VaccinesGenetics and Genomic MedicineGenome Editing and Genome RegulationGenome Engineering and DNA repairIn Situ Gene EditingIn Vitro Genetic DepletionIn Vivo Gene EditingLocus StructureMolecular EpigeneticsNano-TherapyOff-Target EffectsOptimizing Repair of CRISPR-Generated DNA BreaksProgrammable Gene ExpressionRegulatory, Safety Aspects of Cell and Gene TherapyRepeated SequencesRNA Editing TechnologyRNA Guided Nuclease for Genome ModificationsRNAi and Gene TherapyRNAi based Screening TechnologiesSingle Base EditingSpacer Acquisition, Biogenesis, and InterferenceTargeted Gene ReplacementVectors for Gene TherapyViral Gene Therapy